Nishida Y, Hata M, Ayaki T, Ryo H, Yamagata M, Shimizu K, Nishizuka Y
Molecular Biology Unit, Aichi Cancer Center Research Institute, Nagoya, Japan.
EMBO J. 1988 Mar;7(3):775-81. doi: 10.1002/j.1460-2075.1988.tb02875.x.
The genomic and cDNA fragments of Drosophila melanogaster, homologous to human c-raf-1, were cloned. The nucleotide sequence predicted the primary structure of a polypeptide of 666 amino acid residues with a highly conserved Ser-Thr kinase domain on its carboxy terminal half. Draf-1 was mapped to the 2F region of the X chromosome. Two newly induced recessive lethals belonging to a complementation group in this region were identified to be defective in Draf-1 by P element-mediated rescue experiments. The mutants die at larval/pupal stages. The mutant larvae are apparently normal, but they harbor serious defects in the organs containing proliferating cells of both somatic and germ line origins. Maternal effects on embryogenesis indicated that Draf-1 is also required in early larval development.
克隆了与人类c-raf-1同源的黑腹果蝇基因组片段和cDNA片段。核苷酸序列预测了一个由666个氨基酸残基组成的多肽的一级结构,其羧基末端一半具有高度保守的丝氨酸-苏氨酸激酶结构域。Draf-1定位于X染色体的2F区域。通过P因子介导的拯救实验,确定该区域属于一个互补群的两个新诱导的隐性致死突变体在Draf-1中存在缺陷。这些突变体在幼虫/蛹期死亡。突变体幼虫表面看似正常,但在含有体细胞和生殖系来源增殖细胞的器官中存在严重缺陷。对胚胎发育的母体影响表明,Draf-1在幼虫早期发育中也是必需的。